Quinn Patrick, Bowers Robert M, Zhang Xiaoyu, Wahlund Thomas M, Fanelli Michael A, Olszova Daniela, Read Betsy A
Department of Biological Sciences, California State University-San Marcos, San Marcos, CA 92078, USA.
Appl Environ Microbiol. 2006 Aug;72(8):5512-26. doi: 10.1128/AEM.00343-06.
Marine unicellular coccolithophore algae produce species-specific calcite scales otherwise known as coccoliths. While the coccoliths and their elaborate architecture have attracted the attention of investigators from various scientific disciplines, our knowledge of the underpinnings of the process of biomineralization in this alga is still in its infancy. The processes of calcification and coccolithogenesis are highly regulated and likely to be complex, requiring coordinated expression of many genes and pathways. In this study, we have employed cDNA microarrays to investigate changes in gene expression associated with biomineralization in the most abundant coccolithophorid, Emiliania huxleyi. Expression profiling of cultures grown under calcifying and noncalcifying conditions has been carried out using cDNA microarrays corresponding to approximately 2,300 expressed sequence tags. A total of 127 significantly up- or down-regulated transcripts were identified using a P value of 0.01 and a change of >2.0-fold. Real-time reverse transcriptase PCR was used to test the overall validity of the microarray data, as well as the relevance of many of the proteins predicted to be associated with biomineralization, including a novel gamma-class carbonic anhydrase (A. R. Soto, H. Zheng, D. Shoemaker, J. Rodriguez, B. A. Read, and T. M. Wahlund, Appl. Environ. Microbiol. 72:5500-5511, 2006). Differentially regulated genes include those related to cellular metabolism, ion channels, transport proteins, vesicular trafficking, and cell signaling. The putative function of the vast majority of candidate transcripts could not be defined. Nonetheless, the data described herein represent profiles of the transcription changes associated with biomineralization-related pathways in E. huxleyi and have identified novel and potentially useful targets for more detailed analysis.
海洋单细胞颗石藻会产生物种特异性的方解石鳞片,即所谓的颗石。虽然颗石及其精巧的结构吸引了来自不同科学领域研究人员的关注,但我们对这种藻类生物矿化过程的基础认知仍处于起步阶段。钙化和颗石形成过程受到高度调控,且可能很复杂,需要许多基因和途径的协调表达。在本研究中,我们利用cDNA微阵列来研究与最丰富的颗石藻——赫氏艾氏藻生物矿化相关的基因表达变化。使用对应约2300个表达序列标签的cDNA微阵列,对在钙化和非钙化条件下生长的培养物进行了表达谱分析。使用P值0.01和变化>2.0倍的标准,共鉴定出127个显著上调或下调的转录本。实时逆转录PCR用于测试微阵列数据的整体有效性,以及许多预测与生物矿化相关的蛋白质的相关性,包括一种新型γ类碳酸酐酶(A.R.索托、H.郑、D.休梅克、J.罗德里格斯、B.A.里德和T.M.瓦伦德,《应用与环境微生物学》72:5500 - 5511, 2006)。差异调节的基因包括与细胞代谢、离子通道、转运蛋白、囊泡运输和细胞信号传导相关的基因。绝大多数候选转录本的推定功能无法确定。尽管如此,本文所述数据代表了赫氏艾氏藻中与生物矿化相关途径的转录变化谱,并确定了用于更详细分析的新的且可能有用的靶点。